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The bacterial iron sensor IdeR recognizes its DNA targets by indirect readout
The iron-dependent regulator IdeR is the main transcriptional regulator controlling iron homeostasis genes in Actinobacteria, including species from the Corynebacterium, Mycobacterium and Streptomyces genera, as well as the erythromycin-producing bacterium Saccharopolyspora erythraea. Despite being...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8464063/ https://www.ncbi.nlm.nih.gov/pubmed/34417623 http://dx.doi.org/10.1093/nar/gkab711 |
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author | Marcos-Torres, Francisco Javier Maurer, Dirk Juniar, Linda Griese, Julia J |
author_facet | Marcos-Torres, Francisco Javier Maurer, Dirk Juniar, Linda Griese, Julia J |
author_sort | Marcos-Torres, Francisco Javier |
collection | PubMed |
description | The iron-dependent regulator IdeR is the main transcriptional regulator controlling iron homeostasis genes in Actinobacteria, including species from the Corynebacterium, Mycobacterium and Streptomyces genera, as well as the erythromycin-producing bacterium Saccharopolyspora erythraea. Despite being a well-studied transcription factor since the identification of the Diphtheria toxin repressor DtxR three decades ago, the details of how IdeR proteins recognize their highly conserved 19-bp DNA target remain to be elucidated. IdeR makes few direct contacts with DNA bases in its target sequence, and we show here that these contacts are not required for target recognition. The results of our structural and mutational studies support a model wherein IdeR mainly uses an indirect readout mechanism, identifying its targets via the sequence-dependent DNA backbone structure rather than through specific contacts with the DNA bases. Furthermore, we show that IdeR efficiently recognizes a shorter palindromic sequence corresponding to a half binding site as compared to the full 19-bp target previously reported, expanding the number of potential target genes controlled by IdeR proteins. |
format | Online Article Text |
id | pubmed-8464063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-84640632021-09-27 The bacterial iron sensor IdeR recognizes its DNA targets by indirect readout Marcos-Torres, Francisco Javier Maurer, Dirk Juniar, Linda Griese, Julia J Nucleic Acids Res Structural Biology The iron-dependent regulator IdeR is the main transcriptional regulator controlling iron homeostasis genes in Actinobacteria, including species from the Corynebacterium, Mycobacterium and Streptomyces genera, as well as the erythromycin-producing bacterium Saccharopolyspora erythraea. Despite being a well-studied transcription factor since the identification of the Diphtheria toxin repressor DtxR three decades ago, the details of how IdeR proteins recognize their highly conserved 19-bp DNA target remain to be elucidated. IdeR makes few direct contacts with DNA bases in its target sequence, and we show here that these contacts are not required for target recognition. The results of our structural and mutational studies support a model wherein IdeR mainly uses an indirect readout mechanism, identifying its targets via the sequence-dependent DNA backbone structure rather than through specific contacts with the DNA bases. Furthermore, we show that IdeR efficiently recognizes a shorter palindromic sequence corresponding to a half binding site as compared to the full 19-bp target previously reported, expanding the number of potential target genes controlled by IdeR proteins. Oxford University Press 2021-08-20 /pmc/articles/PMC8464063/ /pubmed/34417623 http://dx.doi.org/10.1093/nar/gkab711 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Structural Biology Marcos-Torres, Francisco Javier Maurer, Dirk Juniar, Linda Griese, Julia J The bacterial iron sensor IdeR recognizes its DNA targets by indirect readout |
title | The bacterial iron sensor IdeR recognizes its DNA targets by indirect readout |
title_full | The bacterial iron sensor IdeR recognizes its DNA targets by indirect readout |
title_fullStr | The bacterial iron sensor IdeR recognizes its DNA targets by indirect readout |
title_full_unstemmed | The bacterial iron sensor IdeR recognizes its DNA targets by indirect readout |
title_short | The bacterial iron sensor IdeR recognizes its DNA targets by indirect readout |
title_sort | bacterial iron sensor ider recognizes its dna targets by indirect readout |
topic | Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8464063/ https://www.ncbi.nlm.nih.gov/pubmed/34417623 http://dx.doi.org/10.1093/nar/gkab711 |
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